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Items: 1 to 20 of 143

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093377copy number variation1nstd102humannot provided GRCh37 chr4: 154,928,902-155,707,223 , GRCh38.p12 chr4|NW_017363814.1: 1-420,675 , GRCh38.p12 chr4: 154,007,750-154,786,071 FGA, FGG, 13 more genes
    nsv7057108inversion1nstd229human GRCh38 chr4: 154,728,774-156,655,899 , GRCh37.p13 chr4: 155,649,926-157,577,051 RNU2-66P, LOC105377501, 38 more genes
    nsv7048230inversion1nstd229human GRCh38 chr4: 149,781,104-157,324,460 , GRCh37.p13 chr4: 150,702,256-158,245,612 LOC107986197, LINC02273, 119 more genes
    nsv6756021copy number variation1nstd229human GRCh38 chr4: 154,703,230-154,758,289 , GRCh37.p13 chr4: 155,624,382-155,679,441 LRAT, NDUFB2P1
    nsv6752708copy number variation1nstd229human GRCh38 chr4: 154,489,292-154,803,489 , GRCh37.p13 chr4: 155,410,444-155,724,641 PLRG1, LOC105377500, 12 more genes
    nsv6750817copy number variation1nstd229human GRCh38 chr4: 154,013,779-154,793,137 , GRCh37.p13 chr4: 154,934,931-155,714,289 LRAT, RBM46, 14 more genes
    nsv6741165copy number variation1nstd229human GRCh38 chr4: 154,751,402-154,757,405 , GRCh37.p13 chr4: 155,672,554-155,678,557 LRAT
    nsv6740088copy number variation1nstd229human GRCh38 chr4: 154,739,542-154,739,584 , GRCh37.p13 chr4: 155,660,694-155,660,736 LRAT
    nsv6739313copy number variation1nstd229human GRCh38 chr4: 154,558,116-154,773,277 , GRCh37.p13 chr4: 155,479,268-155,694,429 LOC105377500, FGA, 4 more genes
    nsv6380508copy number variation1nstd223human GRCh38 chr4: 154,726,601-154,805,200 , GRCh37.p13 chr4: 155,647,753-155,726,352 RNU2-66P, RBM46, 3 more genes
    nsv6135300copy number variation1nstd213human GRCh37 chr4: 155,580,000-155,860,001 , GRCh38.p12 chr4: 154,658,848-154,938,849 LRAT, RBM46, 4 more genes
    nsv6134911copy number variation1nstd213human GRCh37 chr4: 147,270,000-190,610,001 , GRCh38.p12 chr4: 146,348,848-189,688,847 , AGA, 517 more genes
    nsv6134884copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,720,001 , GRCh38.p12 chr4: 108,308,844-160,798,849 , ANK2, 616 more genes
    nsv6134731copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,710,001 , GRCh38.p12 chr4: 108,308,844-160,788,849 , ANK2, 616 more genes
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5169580mobile element insertion1nstd203human GRCh38 chr4: 154,750,848-154,750,865 , GRCh37.p13 chr4: 155,672,000-155,672,017 LRAT
    nsv4929770copy number variation1nstd200human GRCh38 chr4: 154,751,402-154,757,402 , GRCh37.p13 chr4: 155,672,554-155,678,554 LRAT
    nsv4929769copy number variation1nstd200human GRCh38 chr4: 154,743,164-154,744,279 , GRCh37.p13 chr4: 155,664,316-155,665,431 LRAT
    nsv4801222copy number variation1nstd200human GRCh37 chr4: 155,672,554-155,678,554 , GRCh38.p12 chr4: 154,751,402-154,757,402 LRAT
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